Johanna Schleutker
occupation: researcher
Articles 157
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Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
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The interactome of the prostate-specific protein Anoctamin 7
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Inherited DNA Repair Gene Mutations in Men with Lethal Prostate Cancer
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The effect of sample size on polygenic hazard models for prostate cancer
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A genetic risk score to personalize prostate cancer screening, applied to population data
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ShAn: An easy-to-use tool for interactive and integrated variant annotation
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Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer
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Prostate cancer risk prediction using a polygenic risk score
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The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor
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Whole-exome sequencing of Finnish patients with vascular cognitive impairment
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Risk Prediction of Prostate Cancer with Single Nucleotide Polymorphisms (SNPs) and Prostate-Specific Antigen (PSA)
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Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry
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Shared heritability and functional enrichment across six solid cancers
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Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
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Oligogenic basis of sporadic ALS: The example of p.Ala90Val mutation
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Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
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Publisher Correction: Shared heritability and functional enrichment across six solid cancers
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ANO7 rs77559646 Is Associated With First-line Docetaxel Treatment Response in Metastatic Castration-resistant Prostate Cancer
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Recurrent moderate-risk mutations in Finnish breast and ovarian cancer patients
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Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
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Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.
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Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
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Circulating Metabolic Biomarkers of Screen-Detected Prostate Cancer in the ProtecT Study
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Germline variation at 8q24 and prostate cancer risk in men of European ancestry
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Synergistic Interaction of HOXB13 and CIP2A Predisposes to Aggressive Prostate Cancer
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AA9int: SNP interaction pattern search using non-hierarchical additive model set
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ANO7 is associated with aggressive prostate cancer
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Biology and Clinical Implications of the 19q13 Aggressive Prostate Cancer Susceptibility Locus
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Shared heritability and functional enrichment across six solid cancers
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Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases.
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Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts.
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Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility
Human - wd:Q42590313